Exploring cation distribution in ion-exchanged Al,Ga-containing metal-organic frameworks using 17O NMR spectroscopy
Abstract
A mixed-metal metal–organic framework, (Al,Ga)-MIL-53, synthesised by post-synthetic ion exchange has been investigated using solid-state nuclear magnetic resonance (NMR) spectroscopy, microscopy and energy dispersive X-ray (EDX) spectroscopy. 17O enrichment during the ion-exchange process enables site specific information on the metal distribution to be obtained. Within this work two ion-exchange processes have been explored. In the first approach (exchange of metals in the framework with dissolved metal salts), 17O NMR spectroscopy reveals the formation of crystallites with a core–shell structure, where the cation exchange takes place on the surface of these materials forming a shell with a roughly equal ratio of Al3+ and Ga3+. For the second approach (exchange of metals between two frameworks), no core–shell structure is observed, and instead crystallites containing a majority of Al3+ are obtained with lower levels of Ga3+. Noticeably, these particles show little variation in the metal cation distribution between crystallites, a result not previously observed for bulk (Al,Ga)-MIL-53 materials. In all cases where ion exchange has taken place NMR spectroscopy reveals a slight preference for clustering of like cations.
Citation
Davis , Z H , Morris , R E & Ashbrook , S E 2023 , ' Exploring cation distribution in ion-exchanged Al,Ga-containing metal-organic frameworks using 17 O NMR spectroscopy ' , Physical Chemistry Chemical Physics , vol. 25 , no. 30 , pp. 20267-20280 . https://doi.org/10.1039/D3CP03071G
Publication
Physical Chemistry Chemical Physics
Status
Peer reviewed
ISSN
1463-9076Type
Journal article
Rights
Copyright © 2023 The Author(s). This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (https://creativecommons.org/licenses/by/3.0/).
Description
The authors would like to thank the ERC (Advanced Grant 787073 ADOR) for support. The UK High-Field Solid-State NMR Facility used in this research was funded by EPSRC and BBSRC (EP/T015063/1), in addition to (for results at 850 MHz) he University of Warwick including via part funding through Birmingham Science City Advanced Materials Projects 1 and 2 supported by Advantage West Midlands (AWM) and the European Regional Development Fund (ERDF), and for the 1 GHz instrument, (EP/R029946/1). Collaborative assistance from the Facility Manager Team (Dr Trent Franks, University of Warwick) is acknowledged. The Jeol JSM-IT200 SEM used in this research was supported by the EPSRC Light Element Analysis Facility Grant (EP/T019298/1) and the EPSRC Strategic Equipment Resource Grant (EP/R023751/1). Collaborative assistance from Dr David Miller (University of St Andrews) is acknowledged.Collections
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